The FDA recommends implementing a coding standard during medical device software development. In practice, this means running a static analysis tool to detect any problematic constructs that could lead to problems down the road.
But if you think you can simply download an analyzer and go, you might consider that the FDA requires documented details associated with code quality activities.
What standard are you going to check against? What rules in the analyzer cover the standard? Which rules are you suppressing? The implementation of static analysis is enough to cause headaches, gastrointestinal discomfort, and other side-effects.
This webinar prescribes some static analysis implementation best practices to relieve your FDA compliance symptoms, including:
The benefits of static analysis and what to look for in an analyzer
How to automate static analysis execution
How to integrate static analysis within your software development processes.
How to reduce noise and stop wasting time manually triaging results
ISO 62304: Defines processes that are required in any given SDLC to ensure that it compiles with the creation or maintenance medical device software
Andy Stopford has over 16 years experience leading teams to deliver pioneering software solutions that enable business goals to be achieved. With experience drawn from the e-commerce, financial, insurance, banking and healthcare sectors he is committed to creating quality software that adheres to best practices and delivers solutions that are robust and help clients achieve business goals.
Andy is a software engineer by trade and is a published book author and keen writer with 200 magazine and journal articles over his career. He has a great depth and breadth of knowledge in a variety of technologies and is passionate about all things software engineering.
Andy leads the HAVAS HEALTH SOFTWARE team of software engineers to develop solutions that focus on the best possible outcome for the end user that ensure the business needs are met.
@andystopford
The FDA recommends implementing a coding standard during medical device software development. In practice, this means running a static analysis tool to detect any problematic constructs that could lead to problems down the road. But if you think you can simply download an analyzer and go, you might consider that the FDA requires documented details associated with code quality activities. What standard are you going to check against? What rules in the analyzer cover the standard? Which rules are you suppressing? The implementation of static analysis is enough to cause headaches, gastrointestinal discomfort, and other side-effects. In these webinar slides, we’ll prescribe some static analysis implementation best practices to relieve your FDA compliance symptoms, including:
• The benefits of static analysis and what to look for in an analyzer
• How to automate static analysis execution
• How to integrate static analysis within your software development processes.
• How to reduce noise and stop wasting time manually triaging results
Death by documentation - Medical Device Development ChallengesAligned AG
“Writing documents and putting them into binders does not sound like rocket science.”
Nevertheless, many of us have experienced how documentation and traceability according to ISO 13485 and FDA QSR 820 turns into a both complex and cumbersome activity. Surprisingly enough, as long as regulatory demands are met, the documentation process itself is seldom scrutinized for efficiency improvements.
This presentation highlights how great savings can be made in this area. We uncover bad documentation practices, their consequences and potential remedies with the intent to make the medical device documentation process more efficient.
Driving Risks Out of Embedded Automotive SoftwareParasoft
Automobiles are becoming the ultimate mobile computer. Popular models have as many as 100 Electronic Control Units (ECUs), while high-end models push 200 ECUs. Those processors run hundreds of millions of lines of code written by the OEMs’ teams and external contractors—often for black-box assemblies. Modern cars also have increasingly sophisticated high-bandwidth internal networks and unprecedented external connectivity. Considering that no code is 100% error-free, these factors point to an unprecedented need to manage the risks of failure—including protecting life and property, avoiding costly recalls, and reducing the risk of ruinous lawsuits.
ISO 62304: Defines processes that are required in any given SDLC to ensure that it compiles with the creation or maintenance medical device software
Andy Stopford has over 16 years experience leading teams to deliver pioneering software solutions that enable business goals to be achieved. With experience drawn from the e-commerce, financial, insurance, banking and healthcare sectors he is committed to creating quality software that adheres to best practices and delivers solutions that are robust and help clients achieve business goals.
Andy is a software engineer by trade and is a published book author and keen writer with 200 magazine and journal articles over his career. He has a great depth and breadth of knowledge in a variety of technologies and is passionate about all things software engineering.
Andy leads the HAVAS HEALTH SOFTWARE team of software engineers to develop solutions that focus on the best possible outcome for the end user that ensure the business needs are met.
@andystopford
The FDA recommends implementing a coding standard during medical device software development. In practice, this means running a static analysis tool to detect any problematic constructs that could lead to problems down the road. But if you think you can simply download an analyzer and go, you might consider that the FDA requires documented details associated with code quality activities. What standard are you going to check against? What rules in the analyzer cover the standard? Which rules are you suppressing? The implementation of static analysis is enough to cause headaches, gastrointestinal discomfort, and other side-effects. In these webinar slides, we’ll prescribe some static analysis implementation best practices to relieve your FDA compliance symptoms, including:
• The benefits of static analysis and what to look for in an analyzer
• How to automate static analysis execution
• How to integrate static analysis within your software development processes.
• How to reduce noise and stop wasting time manually triaging results
Death by documentation - Medical Device Development ChallengesAligned AG
“Writing documents and putting them into binders does not sound like rocket science.”
Nevertheless, many of us have experienced how documentation and traceability according to ISO 13485 and FDA QSR 820 turns into a both complex and cumbersome activity. Surprisingly enough, as long as regulatory demands are met, the documentation process itself is seldom scrutinized for efficiency improvements.
This presentation highlights how great savings can be made in this area. We uncover bad documentation practices, their consequences and potential remedies with the intent to make the medical device documentation process more efficient.
Driving Risks Out of Embedded Automotive SoftwareParasoft
Automobiles are becoming the ultimate mobile computer. Popular models have as many as 100 Electronic Control Units (ECUs), while high-end models push 200 ECUs. Those processors run hundreds of millions of lines of code written by the OEMs’ teams and external contractors—often for black-box assemblies. Modern cars also have increasingly sophisticated high-bandwidth internal networks and unprecedented external connectivity. Considering that no code is 100% error-free, these factors point to an unprecedented need to manage the risks of failure—including protecting life and property, avoiding costly recalls, and reducing the risk of ruinous lawsuits.
Arthur Hicken Chief Evangelist of Parasoft @ PSQT 2016 discusses:
• What the shift from automated to
continuous means
• How disruption requires changes to how
we test software
• Addressing gaps between Dev and Ops
• Technologies that enable Continuous
General Principals Of Software Validationstaciemarotta
This guidance outlines general validation principles that the Food and Drug Administration (FDA)
considers to be applicable to the validation of medical device software or the validation of software
used to design, develop, or manufacture medical devices. This final guidance document, Version 2.0,
supersedes the draft document, General Principles of Software Validation, Version 1.1, dated June
9, 1997.
Application Security in a DevOps World: Three Methods for Shifting Left Operations has always resided clearly outside of development. Release candidates are tossed over the fence by development and operations was expected to “just make it work.” The same can be said about many other activities, including application security. This isn’t intended to be derision aimed at development—it’s just a feature of how processes have historically been demarcated. But with the emergence of the DevOps movement, organizations are beginning to apply the “shift-left” principle associated with early testing toward other facets of application development. Security, which has been treated as something you can test into an application, should be built into an application according to DevOps principles. In this presentation, we discuss how to get development and operations working together to build security into the application. We’ll outline three methods and discuss their merits and drawbacks:
• Penetration testing: This is the approach most commonly used.
• Hybrid testing: By applying flow (dynamic analysis) early in the process, you can that look for possible paths through the code that lead to security flaws.
• Preventative testing: By taking a standards-based approach and implementing a set of activities that target defects that lead to security vulnerabilities, you are able to get ahead of security issues that diminish the effectiveness of DevOps approaches.
Norse Live Attack Map http://map.ipviking.com/
8,000,000 sensors in 200 data centers in 50 countries – designed to look like everything
The top 5,000,000 worst IPs on the internet
"There are very rarely attacks against Canada, for whatever reason. I guess they're just too nice."
See also http://www.digitalattackmap.com/#anim=1&color=0&country=ALL&list=0&time=16447&view=map for DDOS live
Presentation describes the importance of IT validation from the perspectives of the FDA and our company. It explains GAMP 5, the Validation Life Cycle, good documentation practices, document naming conventions, Change Control, Problem Management, Periodic Evaluation, FDA 483 Warning Letters and 21 CFR Part 11 and a unique Validation Life Cycle.
Evolving from Automated to Continous Testing for Agile and DevOpsParasoft
As agile development practices mature and DevOps principles begin to infiltrate our corporate cultures, organizations realize the distinct opportunity to accelerate software delivery.
Deploy + Destroy Complete Test EnvironmentsParasoft
This presentation, given at STAREAST in May 2016, explains how Service Virtualization, Containers, and Cloud help organizations test applications on their own terms.
Process and Regulated Processes Software Validation ElementsArta Doci
Medical device manufacturers operate in a competitive marketplace with increasing end-user demands for features and usability and in a highly regulated environment.
Regulatory bodies look for evidence that medical devices are developed under a structured, quality-oriented development process. By following software validation and verification best practices, one can not only increase the likelihood that they will meet their compliance goals, they can also enhance developer productivity.
This presentation is about the validation of software. It focus on the validation of software used in pharmacy. It contains definition of validation, computer system and validation of computer system. It explains the models which are used for software validation and on example i.e. HPLC software validation.
This Presentation gives an idea about validation and different type of validation and overview of computer system/software validation and basics steps for computer system validations as per the regulatory and user requirement specifications.
In this presentation, Adrian Hunt, Pre-Sales Consultant at PRQA explains how to achieve ISO 26262 Compliance with our static analysis tools QA·C and QA·C++.
An introduction to Life Sciences Computer System Validation, applicable regulation, SDLC phases, software categorisation, risk/ change/ deviation management, validation deliverable, risk based approach, regulatory inspection, audit findings, causes of compliance failure, key concepts in CSV etc.
Increasing Efficiency of ISO 26262 Verification and Validation by Combining F...RAKESH RANA
Increasing Efficiency of ISO 26262 Verification and Validation by Combining Fault Injection and Mutation Testing with Model Based Development
Presented at:
8th International Joint Conference on Software Technologies, ICSOFT-EA, Reykjavík, Iceland, 2013
Get full text of publication at:
http://rakeshrana.website/index.php/work/publications/
Accelerate Agile Development with Service Virtualization - Czech TestParasoft
Process deadlocks are endemic to parallel and Agile development environments, where different teams are simultaneously working on interconnected system components—and each team needs to access the others' components in order to complete its own tasks. But when a team ends up waiting for access to dependencies, agility is stifled. One way to break free of these constraints is to use service virtualization to simulate interactions between the application under test and the dependencies that are unavailable or difficult-to-access for dev/test purposes. This presentation explains how service virtualization can help you eliminate the delays created by unavailable and evolving dependencies so you can save time, money, and effort. It will also share case studies that show specific cases where service virtualization helped organizations compress their testing cycles to keep pace with the demands of Agile development.
Arthur Hicken Chief Evangelist of Parasoft @ PSQT 2016 discusses:
• What the shift from automated to
continuous means
• How disruption requires changes to how
we test software
• Addressing gaps between Dev and Ops
• Technologies that enable Continuous
General Principals Of Software Validationstaciemarotta
This guidance outlines general validation principles that the Food and Drug Administration (FDA)
considers to be applicable to the validation of medical device software or the validation of software
used to design, develop, or manufacture medical devices. This final guidance document, Version 2.0,
supersedes the draft document, General Principles of Software Validation, Version 1.1, dated June
9, 1997.
Application Security in a DevOps World: Three Methods for Shifting Left Operations has always resided clearly outside of development. Release candidates are tossed over the fence by development and operations was expected to “just make it work.” The same can be said about many other activities, including application security. This isn’t intended to be derision aimed at development—it’s just a feature of how processes have historically been demarcated. But with the emergence of the DevOps movement, organizations are beginning to apply the “shift-left” principle associated with early testing toward other facets of application development. Security, which has been treated as something you can test into an application, should be built into an application according to DevOps principles. In this presentation, we discuss how to get development and operations working together to build security into the application. We’ll outline three methods and discuss their merits and drawbacks:
• Penetration testing: This is the approach most commonly used.
• Hybrid testing: By applying flow (dynamic analysis) early in the process, you can that look for possible paths through the code that lead to security flaws.
• Preventative testing: By taking a standards-based approach and implementing a set of activities that target defects that lead to security vulnerabilities, you are able to get ahead of security issues that diminish the effectiveness of DevOps approaches.
Norse Live Attack Map http://map.ipviking.com/
8,000,000 sensors in 200 data centers in 50 countries – designed to look like everything
The top 5,000,000 worst IPs on the internet
"There are very rarely attacks against Canada, for whatever reason. I guess they're just too nice."
See also http://www.digitalattackmap.com/#anim=1&color=0&country=ALL&list=0&time=16447&view=map for DDOS live
Presentation describes the importance of IT validation from the perspectives of the FDA and our company. It explains GAMP 5, the Validation Life Cycle, good documentation practices, document naming conventions, Change Control, Problem Management, Periodic Evaluation, FDA 483 Warning Letters and 21 CFR Part 11 and a unique Validation Life Cycle.
Evolving from Automated to Continous Testing for Agile and DevOpsParasoft
As agile development practices mature and DevOps principles begin to infiltrate our corporate cultures, organizations realize the distinct opportunity to accelerate software delivery.
Deploy + Destroy Complete Test EnvironmentsParasoft
This presentation, given at STAREAST in May 2016, explains how Service Virtualization, Containers, and Cloud help organizations test applications on their own terms.
Process and Regulated Processes Software Validation ElementsArta Doci
Medical device manufacturers operate in a competitive marketplace with increasing end-user demands for features and usability and in a highly regulated environment.
Regulatory bodies look for evidence that medical devices are developed under a structured, quality-oriented development process. By following software validation and verification best practices, one can not only increase the likelihood that they will meet their compliance goals, they can also enhance developer productivity.
This presentation is about the validation of software. It focus on the validation of software used in pharmacy. It contains definition of validation, computer system and validation of computer system. It explains the models which are used for software validation and on example i.e. HPLC software validation.
This Presentation gives an idea about validation and different type of validation and overview of computer system/software validation and basics steps for computer system validations as per the regulatory and user requirement specifications.
In this presentation, Adrian Hunt, Pre-Sales Consultant at PRQA explains how to achieve ISO 26262 Compliance with our static analysis tools QA·C and QA·C++.
An introduction to Life Sciences Computer System Validation, applicable regulation, SDLC phases, software categorisation, risk/ change/ deviation management, validation deliverable, risk based approach, regulatory inspection, audit findings, causes of compliance failure, key concepts in CSV etc.
Increasing Efficiency of ISO 26262 Verification and Validation by Combining F...RAKESH RANA
Increasing Efficiency of ISO 26262 Verification and Validation by Combining Fault Injection and Mutation Testing with Model Based Development
Presented at:
8th International Joint Conference on Software Technologies, ICSOFT-EA, Reykjavík, Iceland, 2013
Get full text of publication at:
http://rakeshrana.website/index.php/work/publications/
Accelerate Agile Development with Service Virtualization - Czech TestParasoft
Process deadlocks are endemic to parallel and Agile development environments, where different teams are simultaneously working on interconnected system components—and each team needs to access the others' components in order to complete its own tasks. But when a team ends up waiting for access to dependencies, agility is stifled. One way to break free of these constraints is to use service virtualization to simulate interactions between the application under test and the dependencies that are unavailable or difficult-to-access for dev/test purposes. This presentation explains how service virtualization can help you eliminate the delays created by unavailable and evolving dependencies so you can save time, money, and effort. It will also share case studies that show specific cases where service virtualization helped organizations compress their testing cycles to keep pace with the demands of Agile development.
Parasoft Concerto A complete ALM platform that ensures quality software can b...Engineering Software Lab
Parasoft Concerto is a complete software development management platform that ensures quality software can be produced consistently and efficiently–in any language.
By integrating policy-driven project management with Parasoft Test's quality lifecycle management as well as Parasoft Virtualize's dev/test environment management, Parasoft Concerto ensures predictable project outcomes while driving unprecedented levels of productivity and application quality.
Parasoft delivers a complete framework to create, manage, and extract greater value from unit tests. We help you exercise and test an incomplete system—enabling you to identify problems when they are least difficult, costly, and time-consuming to fix. This reduces the length and cost of downstream processes such as debugging. Moreover, since all tests are written at the unit level, the test suite can be run independent of the complete system. This allows you to isolate code behavior changes, reduces setup complexities, and makes it practical to execute the test suite on a daily basis.
This presentation is about applying test automation to embedded devices. It also contains recommendations on how to handle specific features of embedded devices, such as their “True Real Time” type, a non-PC platforms and absence of a debug port.
Presentation by Yuriy Kozak (Consultant Software Engineer, GlobalLogic, Lviv) and Ihor Semochko (Automation Engineer, GlobalLogic, Lviv), EmbeddedTechTalk, Lviv, 2014.
More details -
http://www.globallogic.com.ua/press-releases/embedded-lviv-techtalk-2-coverage
The medical device industry is facing unprecedented challenges due to emerging technologies and increased regulatory scrutiny.
Current “waterfall” product development methods are ill-suited to dealing with the pace of change and uncertainty that product development organizations are facing. This eBook addresses:
* The shortcomings of waterfall development specifically in regulatory environments.
* How agile development meets the safety, reliability and regulatory needs of the medical device and diagnostics industry.
* How agile development can help ensure delivery of successful software.
Computerized system validation (CSV) as a requirement for good manufacturing ...Ahmed Hasham
The biopharmaceutical industries has more and more used computers to support and accelrate producing of their
products. Computer systems also are accustomed support routine offer of high quality products to boost production
process performance, scale back production prices, and improve product quality. it's vital that these systems square
measure suitable purpose from a business and restrictive perspective. Regulatory authorities treat a lack of regulatory
computer system compliance as a serious GxP deviation.
Computer Software Assurance (CSA): Understanding the FDA’s New Draft GuidanceGreenlight Guru
Understand the FDA's new draft guidance on Computer Software Assurance (CSA).
This presentation originally aired during the 2022 Future of QMS Requirements Virtual Summit.
Better Software East 2016: Evolving Automated to ContinuousParasoft
Evolving from Automated to Continuous Testing
Testing issues can be a significant barrier to taking full advantage of agile approaches to software development and the emerging DevOps movement. To leverage these development and delivery strategies to their fullest, you need to evolve beyond automated testing to continuous testing.
Arthur Hicken discusses the testing and development processes and technology that enable continuous testing. He shares insights on how to close the gap between business expectations and development activities by encapsulating clearly defining development policies for software releases.
Arthur describes how to prevent defects in code and prioritize defect remediation before a release candidate goes live. Explore ways to realistic test environments and simulations—critical features of the dev/test infrastructure—that enable continuous testing.
Learn how to create a feedback loop that exposes defect patterns while highlighting opportunities to improve application design. Take back a comprehensive to do list for processes and infrastructure that must be in place for your organization to implement continuous testing and accelerate the SDLC.
The presentation describes how to conduct reliability planning and testing for software controlled electron-mechanical systems. It is based on working experience in US FDA, FCC and European CE regulated companies. The presentation provides practical and rational steps to improve product reliability and comply with applicable regulations.
研讨会简报介绍了如何进行软件控制的电子机械系统的可靠性规划和测试。它是基于在美国FDA,FCC和欧洲CE规管公司的工作经验。研讨会演示文稿提供仅结合实际,合理的措施来提高产品的可靠性,并遵守适用的法规.
This presentation reviews the regulatory requirements for intended use validation of SaaS-based EDC systems from the Sponsor and CRO perspective and provides best practices for implementing the proper validation in your organization.
Ready, Set, Automate - Best Practices in Using Automated Tools for ValidationCovance
PhUSE/CSS 2019 -- Quality and accuracy are essential in the healthcare industries. Patients and regulators have an expectation that clinical data is accurate, and its analysis is sound. This poster will focus on the general function and benefit these quality control tools can provide and help improve programmers' mundane tasks. This poster will investigate how QC tools can enhance the validation process in varies stages and workflows in different scenarios. Here are a few use cases for automated tools used across pharmaceutical industries, collated based on a portion of a GPP QC process white paper.
This document covers most of the topics in the CSV like Importance of CVS, Why to perform CSV, Validation Deliverables, Part 11 and Annex 11 Diferences
EduQuest Advisory 4 Pillars Of Qsr ComplianceEduQuest, Inc.
FDA believes four core quality subsystems should be the foundation of every firm’s quality efforts. This Advisory, written by Denise Dion, a former FDA investigator and now a Vice President of EduQuest, focuses on what you need to know about Management Controls; Design Controls;Corrective and Preventive Actions (CAPA Systems); and Production and Process Controls (P&PC)-- plus the very important inter-linkages of each.
computer system is a latest validation system in pharmaceutical industries.
To compliance with the good laboratory practice and good manufacturing practice.
it`s part of 211CFR part 11.
Software as a Medical Device (SaMD) Challenges and Opportunities for 2021 and...Greenlight Guru
The SARS-CoV-2 pandemic drastically changes the landscape of digital health innovation. The FDA authorized emergency use for a variety of SaMD products including but not limited to mental health, clinical decision support and remote monitoring software applications. In addition, FDA recently launched the Digital Health Center of Excellence, provided updates on the pre-certification program, and host a session to convey FDA’s current thinking on AI/ML SaMD validation.
SaMD manufacturers must keep up with the fast-evolving regulatory landscape and optimize their software development practices with a goal to demonstrate conformance to the QMS requirements effectively and efficiently.
This presentation originally aired during the 2021 State of Medical Device Virtual Summit.
INFECTION OF THE BRAIN -ENCEPHALITIS ( PPT)blessyjannu21
Neurological system includes brain and spinal cord. It plays an important role in functioning of our body. Encephalitis is the inflammation of the brain. Causes include viral infections, infections from insect bites or an autoimmune reaction that affects the brain. It can be life-threatening or cause long-term complications. Treatment varies, but most people require hospitalization so they can receive intensive treatment, including life support.
ALKAMAGIC PLAN 1350.pdf plan based of door to door delivery of alkaline water...rowala30
Alka magic plan 1350 -we deliver alkaline water at your door step and you can make handsome money by referral programme
we also help and provide systematic guideline to setup 1000 lph alkaline water plant
DECODING THE RISKS - ALCOHOL, TOBACCO & DRUGS.pdfDr Rachana Gujar
Introduction: Substance use education is crucial due to its prevalence and societal impact.
Alcohol Use: Immediate and long-term risks include impaired judgment, health issues, and social consequences.
Tobacco Use: Immediate effects include increased heart rate, while long-term risks encompass cancer and heart disease.
Drug Use: Risks vary depending on the drug type, including health and psychological implications.
Prevention Strategies: Education, healthy coping mechanisms, community support, and policies are vital in preventing substance use.
Harm Reduction Strategies: Safe use practices, medication-assisted treatment, and naloxone availability aim to reduce harm.
Seeking Help for Addiction: Recognizing signs, available treatments, support systems, and resources are essential for recovery.
Personal Stories: Real stories of recovery emphasize hope and resilience.
Interactive Q&A: Engage the audience and encourage discussion.
Conclusion: Recap key points and emphasize the importance of awareness, prevention, and seeking help.
Resources: Provide contact information and links for further support.
Feeding plate for a newborn with Cleft Palate.pptxSatvikaPrasad
A feeding plate is a prosthetic device used for newborns with a cleft palate to assist in feeding and improve nutrition intake. From a prosthodontic perspective, this plate acts as a barrier between the oral and nasal cavities, facilitating effective sucking and swallowing by providing a more normal anatomical structure. It helps to prevent milk from entering the nasal passage, thereby reducing the risk of aspiration and enhancing the infant's ability to feed efficiently. The feeding plate also aids in the development of the oral muscles and can contribute to better growth and weight gain. Its custom fabrication and proper fitting by a prosthodontist are crucial for ensuring comfort and functionality, as well as for minimizing potential complications. Early intervention with a feeding plate can significantly improve the quality of life for both the infant and the parents.
Cold Sores: Causes, Treatments, and Prevention Strategies | The Lifesciences ...The Lifesciences Magazine
Cold Sores, medically known as herpes labialis, are caused by the herpes simplex virus (HSV). HSV-1 is primarily responsible for cold sores, although HSV-2 can also contribute in some cases.
Health Education on prevention of hypertensionRadhika kulvi
Hypertension is a chronic condition of concern due to its role in the causation of coronary heart diseases. Hypertension is a worldwide epidemic and important risk factor for coronary artery disease, stroke and renal diseases. Blood pressure is the force exerted by the blood against the walls of the blood vessels and is sufficient to maintain tissue perfusion during activity and rest. Hypertension is sustained elevation of BP. In adults, HTN exists when systolic blood pressure is equal to or greater than 140mmHg or diastolic BP is equal to or greater than 90mmHg. The
LGBTQ+ Adults: Unique Opportunities and Inclusive Approaches to CareVITASAuthor
This webinar helps clinicians understand the unique healthcare needs of the LGBTQ+ community, primarily in relation to end-of-life care. Topics include social and cultural background and challenges, healthcare disparities, advanced care planning, and strategies for reaching the community and improving quality of care.
Global launch of the Healthy Ageing and Prevention Index 2nd wave – alongside...ILC- UK
The Healthy Ageing and Prevention Index is an online tool created by ILC that ranks countries on six metrics including, life span, health span, work span, income, environmental performance, and happiness. The Index helps us understand how well countries have adapted to longevity and inform decision makers on what must be done to maximise the economic benefits that comes with living well for longer.
Alongside the 77th World Health Assembly in Geneva on 28 May 2024, we launched the second version of our Index, allowing us to track progress and give new insights into what needs to be done to keep populations healthier for longer.
The speakers included:
Professor Orazio Schillaci, Minister of Health, Italy
Dr Hans Groth, Chairman of the Board, World Demographic & Ageing Forum
Professor Ilona Kickbusch, Founder and Chair, Global Health Centre, Geneva Graduate Institute and co-chair, World Health Summit Council
Dr Natasha Azzopardi Muscat, Director, Country Health Policies and Systems Division, World Health Organisation EURO
Dr Marta Lomazzi, Executive Manager, World Federation of Public Health Associations
Dr Shyam Bishen, Head, Centre for Health and Healthcare and Member of the Executive Committee, World Economic Forum
Dr Karin Tegmark Wisell, Director General, Public Health Agency of Sweden
PET CT beginners Guide covers some of the underrepresented topics in PET CTMiadAlsulami
This lecture briefly covers some of the underrepresented topics in Molecular imaging with cases , such as:
- Primary pleural tumors and pleural metastases.
- Distinguishing between MPM and Talc Pleurodesis.
- Urological tumors.
- The role of FDG PET in NET.
Trauma Outpatient Center is a comprehensive facility dedicated to addressing mental health challenges and providing medication-assisted treatment. We offer a diverse range of services aimed at assisting individuals in overcoming addiction, mental health disorders, and related obstacles. Our team consists of seasoned professionals who are both experienced and compassionate, committed to delivering the highest standard of care to our clients. By utilizing evidence-based treatment methods, we strive to help our clients achieve their goals and lead healthier, more fulfilling lives.
Our mission is to provide a safe and supportive environment where our clients can receive the highest quality of care. We are dedicated to assisting our clients in reaching their objectives and improving their overall well-being. We prioritize our clients' needs and individualize treatment plans to ensure they receive tailored care. Our approach is rooted in evidence-based practices proven effective in treating addiction and mental health disorders.